Pith. sign in

REVIEW

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2509.07584 v1 pith:PAATLZP5 submitted 2025-09-09 cond-mat.mtrl-sci

Dispersed multi-walled carbon nanotubes in polyvinyl butyral matrix for transparent ionic conductive films

classification cond-mat.mtrl-sci
keywords carbonnanotubesa-protoncomponentmultiwalledsolventbutyralconductive
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
0 comments
read the original abstract

In this work, we develop methods for increasing the dispersion degree of agglomerated multiwalled carbon nanotubes with subsequent introduction of them into polyvinyl butyral to create transparent conductive films. The influence of proton and a-proton solvents in combination with potassium triiodide (KI3) as a redox component for oxidation of the multiwalled carbon nanotubes surface, which reduces agglomeration due to electrostatic repulsion, is investigated. It is demonstrated that a-proton solvent cyclohexanone ensures a smaller size of the agglomerates (30-300 nm, with a maximum of ~145 nm) compared to proton solvent propyl alcohol (100-3000 nm, with a maximum of ~920 nm). The reduced aggregation is associated with the formation of oxygen-containing functional groups (C=O, C-O, C-O-C, and COO), which increase electrostatic stabilization. The impedance analysis showed that the constant component of the conductivity in the samples with multiwalled carbon nanotubes and a-proton solvent shifts to frequencies of ~104 rad/s after the addition of the redox component, which indicates the formation of ion-conducting channels and stabilization of the jump charge transfer.

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.